{{Rsnum
|rsid = 28933687
|Gene = RP2
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=X
|position=46853726
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RP2
}}{{omim
| id = 312600
| variant = 0006
| desc    = RETINITIS PIGMENTOSA 2, X-LINKED
| rsnum   = 28933687
}}

{{omim
|id=300757
|rsnum=28933687
|variant=0003
}}

{{omim
|id=300757
|rsnum=28933687
|variant=0006
}}

{{ClinVar
|rsid=28933687
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=46713161
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=RP2:6102
|GENE_NAME=RP2
|GENE_ID=6102
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.46713161G>A; NC_000023.10:g.46713161G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300757.0003; 300757.0006
|CLNSIG=5
|CLNCUI=C2681923
|CLNDBN=Retinitis pigmentosa 2
|Disease=Retinitis pigmentosa 2
|CLNACC=RCV000011292.1; RCV000011295.6
|Tags=PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C2681923:312600:791
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}